Cargando…
Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing
Modifications in the tRNA anticodon loop, adjacent to the three-nucleotide anticodon, influence translation fidelity by stabilizing the tRNA to allow for accurate reading of the mRNA genetic code. One example is the N1-methylguanosine modification at guanine nucleotide 37 (m(1)G37) located in the an...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577736/ https://www.ncbi.nlm.nih.gov/pubmed/33016876 http://dx.doi.org/10.7554/eLife.51898 |
_version_ | 1783598236901048320 |
---|---|
author | Hoffer, Eric D Hong, Samuel Sunita, S Maehigashi, Tatsuya Gonzalez, Ruben L Whitford, Paul C Dunham, Christine M |
author_facet | Hoffer, Eric D Hong, Samuel Sunita, S Maehigashi, Tatsuya Gonzalez, Ruben L Whitford, Paul C Dunham, Christine M |
author_sort | Hoffer, Eric D |
collection | PubMed |
description | Modifications in the tRNA anticodon loop, adjacent to the three-nucleotide anticodon, influence translation fidelity by stabilizing the tRNA to allow for accurate reading of the mRNA genetic code. One example is the N1-methylguanosine modification at guanine nucleotide 37 (m(1)G37) located in the anticodon loop andimmediately adjacent to the anticodon nucleotides 34, 35, 36. The absence of m(1)G37 in tRNA(Pro) causes +1 frameshifting on polynucleotide, slippery codons. Here, we report structures of the bacterial ribosome containing tRNA(Pro) bound to either cognate or slippery codons to determine how the m(1)G37 modification prevents mRNA frameshifting. The structures reveal that certain codon–anticodon contexts and the lack of m(1)G37 destabilize interactions of tRNA(Pro) with the P site of the ribosome, causing large conformational changes typically only seen during EF-G-mediated translocation of the mRNA-tRNA pairs. These studies provide molecular insights into how m(1)G37 stabilizes the interactions of tRNA(Pro) with the ribosome in the context of a slippery mRNA codon. |
format | Online Article Text |
id | pubmed-7577736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-75777362020-10-23 Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing Hoffer, Eric D Hong, Samuel Sunita, S Maehigashi, Tatsuya Gonzalez, Ruben L Whitford, Paul C Dunham, Christine M eLife Biochemistry and Chemical Biology Modifications in the tRNA anticodon loop, adjacent to the three-nucleotide anticodon, influence translation fidelity by stabilizing the tRNA to allow for accurate reading of the mRNA genetic code. One example is the N1-methylguanosine modification at guanine nucleotide 37 (m(1)G37) located in the anticodon loop andimmediately adjacent to the anticodon nucleotides 34, 35, 36. The absence of m(1)G37 in tRNA(Pro) causes +1 frameshifting on polynucleotide, slippery codons. Here, we report structures of the bacterial ribosome containing tRNA(Pro) bound to either cognate or slippery codons to determine how the m(1)G37 modification prevents mRNA frameshifting. The structures reveal that certain codon–anticodon contexts and the lack of m(1)G37 destabilize interactions of tRNA(Pro) with the P site of the ribosome, causing large conformational changes typically only seen during EF-G-mediated translocation of the mRNA-tRNA pairs. These studies provide molecular insights into how m(1)G37 stabilizes the interactions of tRNA(Pro) with the ribosome in the context of a slippery mRNA codon. eLife Sciences Publications, Ltd 2020-10-05 /pmc/articles/PMC7577736/ /pubmed/33016876 http://dx.doi.org/10.7554/eLife.51898 Text en © 2020, Hoffer et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry and Chemical Biology Hoffer, Eric D Hong, Samuel Sunita, S Maehigashi, Tatsuya Gonzalez, Ruben L Whitford, Paul C Dunham, Christine M Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing |
title | Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing |
title_full | Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing |
title_fullStr | Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing |
title_full_unstemmed | Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing |
title_short | Structural insights into mRNA reading frame regulation by tRNA modification and slippery codon–anticodon pairing |
title_sort | structural insights into mrna reading frame regulation by trna modification and slippery codon–anticodon pairing |
topic | Biochemistry and Chemical Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7577736/ https://www.ncbi.nlm.nih.gov/pubmed/33016876 http://dx.doi.org/10.7554/eLife.51898 |
work_keys_str_mv | AT hofferericd structuralinsightsintomrnareadingframeregulationbytrnamodificationandslipperycodonanticodonpairing AT hongsamuel structuralinsightsintomrnareadingframeregulationbytrnamodificationandslipperycodonanticodonpairing AT sunitas structuralinsightsintomrnareadingframeregulationbytrnamodificationandslipperycodonanticodonpairing AT maehigashitatsuya structuralinsightsintomrnareadingframeregulationbytrnamodificationandslipperycodonanticodonpairing AT gonzalezrubenl structuralinsightsintomrnareadingframeregulationbytrnamodificationandslipperycodonanticodonpairing AT whitfordpaulc structuralinsightsintomrnareadingframeregulationbytrnamodificationandslipperycodonanticodonpairing AT dunhamchristinem structuralinsightsintomrnareadingframeregulationbytrnamodificationandslipperycodonanticodonpairing |